3-異丁基-1-甲基黃嘌呤,Santa IBMX ,CAS 28822-58-4
- 公司名稱 上?;鄯f生物科技有限公司
- 品牌 Santa Cruz/美國
- 型號(hào)
- 產(chǎn)地 Santa CRUZ
- 廠商性質(zhì) 生產(chǎn)廠家
- 更新時(shí)間 2024/8/11 8:31:51
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3-異丁基-1-甲基黃嘌呤IBMX3-Isobutyl-1-methylxanthine28822-58-4sc-201188
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3-異丁基-1-甲基黃嘌呤,Santa IBMX ,CAS 28822-58-4
產(chǎn)品名稱:3-異丁基-1-甲基黃嘌呤
英文名稱:IBMX
同義詞:3-Isobutyl-1-methylanxthine; Methylisobutylxanthine; MIX
品牌:Santa CRUZ
貨號(hào):sc-201188
CAS號(hào):28822-58-4
純度:≥99%
分子量大?。?22.24
分子式:C10H14N4O2
規(guī)格:200 mg和1 g
貨期:2周
特惠價(jià)格:致電咨詢
英文描述:
IBMX is one of the most potent and nonspecific inhibitors of cyclic nucleotide PDE (phosphodiesterases) with documented IC50 values for PDE1, 2, 3, 4, and 5 equaling 19, 50, 18, 13 and 32. The compound is documented to raise intracellular cyclic AMP levels. In rat sensory neurons the addition of IBMX caused the release of Ca2+ from caffeine ryanodine sensitive internal stores increasing the internal Ca2+ levels and inducing a biphasic membrane current response. Through PDE inhibition IBMX has also inhibited TNFα. IBMX in breast cancer cells has also induced p21 and p27 through a PKA independent pathway. Although a nonspecific PDE inhibitor IBMX does not show inhibition of PDE8B. In neuroendocrine epithelial cells IBMX has been observed to inhibit α-adrenoceptor-mediated 5-HT release at IC50 = 1.3μM.
技術(shù)信息:
物理狀態(tài):Solid
溶解度:Soluble in ethanol (10 mg/ml), DMSO(with gentle warming) (1 M), methanol(warm) (50 mg/ml), 2-propanol, dichloromethane, ether, ethyl acetate, and DMF (~5 mg/ml). Insoluble in water.
存儲(chǔ):Store at room temperature
熔點(diǎn):200-201 °C (lit.)
沸點(diǎn):445.6 °C at 760 mmHg (Predicted)
濃度:1.3 g/cm3 (Predicted)
折射率:n20D 1.57 (Predicted)
IC50: suppresses α-adrenoceptor-mediated 5-HT release: IC50 = 1.3 μM (neuroendocrine epithelial cells); PDE4: IC50 = 13 μM; PDE3: IC50 = 18 μM; PDE1: IC50 = 19 μM; PDE5 : IC50 = 32 μM; PDE2: IC50 = 50 μM; Phosphodiesterase 1B: IC50 = 100 nM (rat); Sodium channel protein type II alpha subunit: IC50 = 1800 nM (human)
Ki數(shù)據(jù):Adenosine A2b receptor: Ki= 50 nM (rat); Adenosine A2a receptor: Ki= 800 nM (rat); Adenosine A1 receptor: Ki= 2000 nM (rat)
pK值:pKa: 8.61 (Predicted), pKb: 1.49 (Predicted)
注意:本產(chǎn)品僅供科研使用。不可用于診斷或治療。
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